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Glioblastoma (GBM) is a common primary central nervous system tumor. Although the multimodal integrated treatment for GBM has made great progress in recent years, the overall survival time of GBM is still short. Thus, novel treatments for GBM are worth further investigation and exploration. This study aimed to investigate the effects of etomidate on GBM tumor growth and the underlying mechanism. A xenograft tumor model was established and treated with etomidate to assess tumor growth. Immunohistochemistry (IHC) assay evaluated the positive rate of Ki67 cells in tumor tissues. Cell counting kit (CCK)-8 and EdU assays accessed the cell viability and proliferation. Immunofluorescence (IF) staining detected the distribution of macrophage markers in tumor tissues. The percentages of M1- and M2-like macrophages in tumor-associated macrophages (TAMs) and co-culture system (macrophages and GBM cells) were detected using flow cytometry. Macrophage polarization-related genes were measured using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Etomidate treatment inhibited the tumor growth, and increased the CD86+ cells but decreased the CD206+ cells in TAMs. The gene expression of M1 markers was increased in TAMs of etomidate-treated mice, whereas that of M2 markers was decreased. Moreover, etomidate treatment increased the number of CD86+ M1-like macrophages co-cultured with tumor cells but decreased that of CD206+ M2-like macrophages, with the upregulation of M1 markers and downregulation of M2 markers. Etomidate inhibited GBM tumor growth by promoting M1 macrophage polarization, suggesting a new insight into the clinical treatment of GBM.
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Neoplasias Encefálicas , Etomidato , Glioblastoma , Macrófagos , Etomidato/farmacología , Glioblastoma/tratamiento farmacológico , Glioblastoma/patología , Glioblastoma/metabolismo , Animales , Ratones , Macrófagos/efectos de los fármacos , Macrófagos/metabolismo , Neoplasias Encefálicas/tratamiento farmacológico , Neoplasias Encefálicas/patología , Neoplasias Encefálicas/metabolismo , Proliferación Celular/efectos de los fármacos , Línea Celular Tumoral , Humanos , Ensayos Antitumor por Modelo de Xenoinjerto , Masculino , Macrófagos Asociados a Tumores/efectos de los fármacos , Macrófagos Asociados a Tumores/metabolismo , Ratones DesnudosRESUMEN
In situ cyclized polyacrylonitrile (CPAN) is developed to replace n-type metal oxide semiconductors (TiO2 or SnO2) as an electron selective layer (ESL) for highly efficient and stable n-i-p perovskite solar cells (PSCs). The CPAN layer is fabricated via facile in situ cyclization reaction of polyacrylonitrile (PAN) coated on a conducting glass substrate. The CPAN layer is robust and insoluble in common solvents, and possesses n-type semiconductor properties with a high electron mobility of 4.13×10-3â cm2 V-1 s-1. With the CPAN as an ESL, the PSC affords a power conversion efficiency (PCE) of 23.12 %, which is the highest for the n-i-p PSCs with organic ESLs. Moreover, the device with the CPAN layer holds superior operational stability, maintaining over 90 % of their initial efficiency after 500â h continuous light soaking. These results confirm that the CPAN layer would be a desirable low-cost and efficient ESL for n-i-p PSCs and other photoelectronic devices with high performance and stability.
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The careful design of nanostructures and multi-compositions of non-noble metal-based electrocatalysts for highly efficient electrocatalytic hydrogen and oxygen evolution reaction (HER and OER) is of great significance to realize sustainable hydrogen release. Herein, bifunctional electrocatalysts of the three-dimensional (3D) cobalt-nickel phosphide nanoarray in situ grown on nickel foams (CoNiP NA/NF) were synthesized through a facile hydrothermal method followed by phosphorization. Due to the unique self-template nanoarray structure and tunable multicomponent system, the CoNiP NA/NF samples present exceptional activity and durability for HER and OER. The optimized sample of CoNiP NA/NF-2 afforded a current density of 10 mA cm-2 at a low overpotential of 162 mV for HER and 499 mV for OER, corresponding with low Tafel slopes of 114.3 and 79.5 mV dec-1, respectively. Density functional theory (DFT) calculations demonstrate that modulation active sites with appropriate electronic properties facilitate the interaction between the catalyst surface and intermediates, especially for the adsorption of absorbed H* and *OOH intermediates, resulting in an optimized energy barrier for HER and OER. The 3D nanoarray structure, with a large specific surface area and abundant ion channels, can enrich the electroactive sites and enhance mass transmission. This work provides novel strategies and insights for the design of robust non-precious metal catalysts.
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Níquel , Agua , Aerosoles , Hidrógeno , Oxígeno , PorosidadRESUMEN
Although composites of organic polymers or n-type small molecule/carbon nanotube (CNT) have achieved significant advances in thermoelectric (TE) applications, p-type TE composites of small organic molecules as thick surface coating layers on the surfaces of inorganic nanoparticles still remain a great challenge. Taking advantage of in situ oxidation reaction of thieno[3,4-b]pyrazine (TP) into TP di-N-oxide (TPNO) on single-walled CNT (SWCNT) surface, a novel synthesis strategy is proposed to achieve flexible films of TE composites with narrow-bandgap (1.19 eV) small molecule coating on SWCNT surface. The TE performance can be effectively enhanced and conveniently tuned by poly(sodium-p-styrenesulfonate) content, TPNO/SWCNT mass ratio, and posttreatment by various polar solvents. The maximum of the composite power factor at room temperature is 29.4 ± 1.0 µW m-1 K-2 . The work presents a way to achieve flexible films of p-type small organic molecule/inorganic composites with clear surface coating morphology for TE application.
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Regulation of peroxymonosulfate (PMS) activation from radical to non-radical pathways is an emerging focus of advanced oxidation processes (AOPs) due to its superiority of anti-interference to complex wastewater. However, the detailed correlation mechanism between the defect structure of the catalyst and the regulation of radicals/non-radicals remains unclear. Herein, natural chalcopyrite (CuFeS2) with different levels of S vacancies created by a simple NaBH4 reduction process was employed to explore the above-mentioned underlying mechanism for constructing high efficiency and low cost of catalyst towards AOPs. With the assistance of simulated solar light, S-deficient chalcopyrite (Sv-NCP) exhibited prominent performance for PMS activation. More interestingly, the different degrees of S vacancies regulated the active species from radicals to non-radical 1O2, thus showing excellent purification of complex wastewater as well as actual pharmaceutical wastewater. Mechanistic analysis reveals that PMS tends to loss electrons on S vacancies sites and is dissociated into 1O2 rather than ·OH/SO4·- due to electron deficiency. Meanwhile, the improved adsorption performance makes the degradation sites of pollutants change from solution to surface. Most importantly, Sv-NCP presented excellent detoxication for antibiotic wastewater due to the high selectivity of 1O2. This work provides novel insights into the regulation of active species in Fenton-like reactions via defect engineering for high efficiency of pollutant degradation.
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With the complexity and diversification of thermoelectric (TE) application scenarios, it becomes increasingly difficult for single-component thermoelectric materials to satisfy practical demands. Therefore, recent researches have largely focused on the development of the multi-component nanocomposites, which are probably a good solution for the TE application of some materials that are not eligible when used alone. In this work, a seires of single-walled carbon nanotube (SWCNT)/polypyrrole (PPy)/tellurium (Te)/lead telluride (PbTe) multi-layer flexible composite films were fabricated via the successive electrodeposition of the flexible PPy layer with a low thermal conductivity, the ultra-thin Te induction layer, and the brittle PbTe layer with a large Seebeck coefficient over the pre-fabricated SWCNT membrane electrode with a high electrical conductivity. Through the complementary advantages between different components and the multiple synergies of the interface engineering, the SWCNT/PPy/Te/PbTe composites harvested the excellent TE performance with a maximum power factor (PF) of 929.8 ± 35.4 µW m-1 K-2 at room temperature, outperforming those of most of the electrochemically-prepared organic/inorganic TE composites reported previously. This work evidenced that the electrochemical multi-layer assembly is a feasible tactic for constructing special thermoelectric materials to meet customized requirements, which could also be applied to other material platforms.
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We report herein the synthesis of a new metal cluster-encapsulated supramolecular capsule, [(C≡C)@Ag(5-6)@(Py6)(2)](CF(3)SO(3))(3-4) (3, Py6 = azacalix[6]pyridine), by use of a bowl-shaped macrocyclic ligand Py6. The multinuclear silver carbide cluster aggregate in 3 is encapsulated by two Py6 ligands through both metal-ligand coordination and cation-π interactions, spotlighting a new synthetic strategy for supramolecular capsules.
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Compuestos de Plata/química , Modelos Moleculares , Estructura Molecular , Espectrometría de Masa por Ionización de ElectrosprayRESUMEN
As one of the most attractive inorganics to improve the thermoelectric (TE) performance of the conducting polymers, tellurium (Te) has received intense concern due to its superior Seebeck coefficient (S). However, far less attention has been paid to polypyrrole (PPy)/Te TE composites to date. In this work, we present an innovative full-electrochemical method to architect PPy/Te TE composite films by sequentially depositing Te with large S and PPy with high electrical conductivity (σ). Consequently, the PPy/Te composite films achieved excellent TE performance, with the largest power factor (PF) reaching up to 234.3 ± 4.1 µW m-1 K-2. To the best of our knowledge, this value approaches the reported highest PF record (240.3 ± 5.0 µW m-1 K-2) for PPy-based composites. This suggests that the modified full-electrochemical method is a feasible and effective strategy for achieving high-performance TE composite films, which would probably provide a general guideline for the design and preparation of excellent TE materials in the future.
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Two-dimensional (2D) layered heterojunctions with a staggered band structure and unique interface properties exhibit promising application prospects in photocatalytic pollutant removal, water splitting, and CO2 reduction. Ultrathin 2D/2D heterojunctions with a large specific surface area and a short migration path of the photogenerated charge always illustrate a better photocatalytic performance than non-ultrathin 2D heterojunction photocatalysts. In this study, a novel ultrathin 2D/2D heterojunction of the Bi2O2(OH)(NO3)/BiOBr nanosheet composite (ultrathin BION/BiOBr) was in situ self-assembled though a cetyltrimethylammonium bromide assisted one-step hydrothermal method. Benefiting from the advantage of the unique ultrathin heterojunction structure, the ultrathin 2D/2D BION/BiOBr heterojunctions exhibit a greatly improved photocatalytic removal effect for multiple pollutants compared to the nanocrystal BION/BiOBr, pure BION. As a representative, the ultrathin 2D/2D Br-modified BION/BiOBr heterojunction shows an enhanced tetracycline degradation rate of 76%, which corresponded to a higher photodegradation rate constant of 0.01116 min-1 when compared to pure BION (17%, 0.00161 min-1) and nanocrystal BION/BiOBr (24%, 0.00223 min-1) under visible-light irradiation for 2 h. A series of characterization and density functional theory calculations demonstrate the enhanced separation and migration efficiency of the photogenerated electrons and holes over the ultrathin heterojunction, facilitating the formation of oxidizing groups for the organic pollutant removal. The possible mechanism of the TC photodegradation and the possible photodegradation pathway are also investigated in detail. This work provides a feasible method for constructing ultrathin 2D/2D heterojunction materials for environmental purification.
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Luz , Tetraciclina , Antibacterianos , Catálisis , Oxidación-ReducciónRESUMEN
Developing a low-cost and efficient photocatalysts activated peroxymonosulfate (PMS) for organic pollutants degradation are recognized as an importance way for dealing with environmental pollution. In this work, Fe-rectorite catalyst was synthesized by a simple impregnation-calcine method to synergetic photo activate PMS for antibiotics degradation. As expected, the Fe-rectorite/PMS/Light system exhibits superior catalytic performance for tetracycline (TC) removal, which achieving 96.4% removal rate of TC (30 mg/L) under light within 60 min. Fe-retorite has better degradation performance for TC than rectorite under photo-mediation. The enhancement of the degradation performance of TC by Fe-retorite can be attributed to the improvement of the separation efficiency of photogenerated electrons and holes in the rectorite by the loading of Fe2O3, and the accelerated active Fe(â ¡)/Fe(â ¢) cycle on the surface under photo-mediation. The large specific surface area and abundant hydroxyl groups of rectorite can also provide active sites for PMS activation. The quenching experiment and electron paramagnetic resonance (EPR) test were indicated that the h+, SO4â¢-, â¢OH, and O2-⢠all contributed to TC degradation. And the possible degradation pathway was proposed by LC-MS. This work helps induced a novel direction that design green, efficient, and recyclable heterogeneous catalysts to synergetic photoinduced PMS activation for enhanced degradation of TC.
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Antibacterianos , Compuestos Férricos , Silicatos de Aluminio , Minerales , PeróxidosRESUMEN
Carbon nitride (C3N4) is a promising metal-free photocatalyst for solar-to-energy conversion, but bulk carbon nitride (BCN) shows insufficient light absorption, sluggish photocarrier transfer and moderate activity for photocatalysis. Herein, a facile strategy to significantly increase solar spectrum absorption of the functionalized porous carbon nitride nanosheets (MFPCN) via molecule self-assembly engineering coupled thermal polymerization is reported. This strategy can greatly enhance the wide-solar-spectrum absorption of MFPCN up to 1000 nm than most reported carbon nitride-based photocatalysts. Experimental characterizations and theoretical calculations together display that this strategy could introduce hydroxyl groups into the structure of MFPCN as well as the rich pores and active sites at the edges of framework, which can narrow the bandgap and accelerate the transfer and separation of photoinduced carries. As a result, the optimal MFPCN photocatalyst exhibit the excellent photocatalytic hydrogen evolution rate of 7.745 mmol g-1h-1 under simulated solar irradiation, which is ≈13 times that of BCN with remarkable durable CO2 reduction activities. New findings in this work will provide an approach to extend solar spectrum absorption of metal-free catalysts for solar fuel cascades.
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Ultrathin two-dimensional (2D) metal oxyhalides exhibit outstanding photocatalytic properties with unique electronic and interfacial structures. Compared with monometallic oxyhalides, bimetallic oxyhalides are less explored. In this work, we have developed a novel top-down wet-chemistry desalination approach to remove the alkali-halide salt layer within the complicated precursor bulk structural matrix Pb0.6Bi1.4Cs0.6O2Cl2, and successfully fabricate a new 2D ultrathin bimetallic oxyhalide Pb0.6Bi1.4O2Cl1.4. The unlocked larger surface area, rich bimetallic active sites, and faster carrier dynamics within Pb0.6Bi1.4O2Cl1.4 layers significantly enhance the photocatalytic efficiency for atmospheric CO2 reduction. It outperforms the corresponding parental matrix phase and other state-of-the-art bismuth-based monometallic oxyhalides photocatalysts. This work reports a top-down desalination strategy to engineering ultrathin bimetallic 2D material for photocatalytic atmospheric CO2 reduction, which sheds light on further constructing other ultrathin 2D catalysts for environmental and energy applications from similar complicate structure matrixes.
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Clarifying the responsibilities and constructing the synergy of different active phases are of great significance but still an urgent challenge for the heterostructure catalyst to improve the hydrogen evolution reaction (HER) process. Here, three-dimensional (3D) CoxNi(1-x)(OH)2 hollow structure integrating MoS2 nanosheet catalysts [CoxNi(1-x)(OH)2@MoS2] were ingeniously designed and prepared. This unique structure has realized the construction of a dual active phase for the optimized stepwise-synergetic hydrogen evolution process over a universal pH range through interface assembly engineering. Meanwhile, the 3D hollow heterostructure with a high surface-to-volume ratio can effectively avoid the agglomeration of MoS2 and enhance the CoxNi(1-x)(OH)2-MoS2 heterointerfaces. Thus, superior HER activity and stability were obtained over the universal pH range. Density functional theory calculation reveals that CoxNi(1-x)(OH)2 and MoS2 phases provide efficient active sites for rate-determining water dissociation and H* adsorption/H2 generation on CoxNi(1-x)(OH)2-MoS2 heterointerfaces, respectively, resulting in an optimized energy barrier for HER. This work proposes a constructive strategy to design highly efficient electrocatalysts based on the heterointerface with a defined responsible active phase of electrocatalysts.
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The designed synthesis and structural characterization of two metal cluster-centered metallosupramolecular architectures are reported. In complex [(CF(3)SO(3))Ag(4)((t)BuC≡C)(Py8)](CF(3)SO(3))(2) (1) and [(CF(3)SO(3))Ag(4){C≡C-(m-C(6)H(4))-C≡C-(m-C(6)H(4))-C≡C-(m-C(6)H(4))-C≡C}Ag(4)(CF(3)SO(3))(Py8)(2)](CF(3)SO(3))(4) (2), organic acetylide ligands are utilized to induce the formation of polynuclear silver aggregates, which are encapsulated into the central cavity of the neutral macrocyclic compound azacalix[8]pyridine (Py8). The tetrasilver cluster centered [2]- and [3]-pseudo-rotaxane structures are obtained and fully characterized by X-ray crystallography, ESI mass spectrometry, and (1)H NMR spectroscopy.
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Rotaxanos/química , Rotaxanos/síntesis química , Plata/química , Cápsulas/química , Cristalografía por Rayos X , Ligandos , Espectroscopía de Resonancia Magnética , Modelos Moleculares , Estructura Molecular , Nanoestructuras/química , Compuestos Organometálicos/síntesis química , Compuestos Organometálicos/química , Espectrometría de Masa por Ionización de ElectrosprayRESUMEN
Organic polymer/inorganic particle composites with thermoelectric (TE) properties have witnessed rapid progress in recent years. Nevertheless, both development of novel polymers and optimization of compositing methods remain highly desirable. In this study, we first demonstrated a simulated in situ coagulation strategy for construction of high-performance thermoelectric materials by utilizing single-walled carbon nanotubes (SWCNTs) and a new D-A polymer TPO-TTP12 that was synthesized via incorporating dioxothiopyrone subunit into a polymeric chain. It was proven that the preparation methods have a significant influence on thermoelectric properties of the TPO-TTP12/SWCNT composites. The in situ prepared composite films tend to achieve much better thermoelectric performances than those prepared by simply mixing the corresponding polymer with SWCNTs. As a result, the in situ compositing obtains the highest Seebeck coefficient of 66.10 ± 0.05 µV K-1 at the TPO-TTP12-to-SWCNT mass ratio of 1/2, and the best electrical conductivity of up to 500.5 ± 53.3 S cm-1 at the polymer/SWCNT mass ratio of 1/20, respectively; moreover, the power factor for the in situ prepared composites reaches a maximum value of 141.94 ± 1.47 µW m-1 K-2, far higher than that of 104.68 ± 0.86 µW m-1 K-2 for the by-mixing produced composites. This indicates that the dioxothiopyrone moiety is a promising building block for constructing thermoelectric polymers, and the simulated in situ compositing strategy is a promising way to improve TE properties of composite materials.
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Solution-processable organic-inorganic hybrid perovskites are being widely investigated for many applications, including solar cells, light-emitting diodes, photodetectors, and lasers. Herein, we report, for the first time, successful fabrication of xerographic photoreceptors using methylammonium lead iodide (CH3NH3PbI3) perovskite as a light-absorbing material. With the incorporation of polyethylene glycol (PEG) into the perovskite film, the ion migration inherent to the perovskite material can be effectively suppressed, and the resulting photoreceptor exhibits a high and panchromatic photosensitivity, large surface potential, low dark decay, and high environmental resistance and electrical cycling stability. Specifically, the energies required to photodischarge one half of the initial surface potential (E 0.5) are 0.074 µJ cm-2 at 550 nm and 0.14 µJ cm-2 at 780 nm, respectively. The photosensitivites outmatch those of the conventionally used organic pigments having narrow spectral responses. Our findings inform a new generation of highly efficient and low-cost xerographic photoreceptors based on perovskite materials.
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It is especially significant to design and construct high-performance and stable three-dimensional (3D) bifunctional nanoarchitecture electrocatalysts toward overall water splitting. Herein, we have constructed 3D self-supported phosphorus-doped ruthenium-cobalt nanowires on nickel foams (RuCoP/NF) via a simple hydrothermal reaction followed by a low-temperature phosphating reaction. Doping P can not merely enhance the intrinsic activity of electrocatalysts for overall water splitting but at the same time increase electrochemical surface areas (ECSAs) to expose more accessible active sites. As a 3D bifunctional catalyst, RuCoP/NF demonstrates superior performance for HER (44 mV@10 mA cm-2) and OER (379 mV@50 mA cm-2) in 1.0 M KOH electrolyte solution. The overall water-splitting system was assembled using RuCoP/NF as both anode and cathode. Besides, it exhibits a voltage of 1.533 V at a current density of 10 mA cm-2 and long-term durability within 24 h. P-dopant changes the electron structure of Ru and Co, which is conducive to the formation of Ruδ- and Coδ+, resulting in the adjustment of binding H*/OH* and the improvement of the overall water-splitting reaction kinetics. This work provides a facile method to produce heteroatom-doped and high-performance catalysts for efficient overall water splitting.
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Objective: To compare the changes in the number of circulating endothelial progenitor cells and hypoxia-inducible factors in patients with type 2 diabetes at different altitudes, and to provide a basis for the research and treatment of type 2 diabetes vascular complications. Methods: Selected Type 2 diabetes patients who were diagnosed in a low altitude area of 386 m (Xianyang City) and a high altitude area of 1 520 m (Lanzhou) (25 persons/29 persons) and healthy persons (20 persons/20 persons) were selected. An automatic biochemical analyzer was used to detect the indexes of blood lipids, blood glucose, and glycosylated hemoglobin of the two groups of people, and the concentration of Hypoxia inducible factor-1α (HIF-1α) was detected by enzyme-linked immunosorbent assay (ELISA). The number of circulating endothelial progenitor cells (EPCs) in peripheral blood was determined by a cytometer. Results: No matter in low or high altitude areas, the number of circulating EPCs in the diabetes group was lower than that in the healthy group (Pï¼0.01). The levels of body mass index (BMI), waist to hip ratio (WHR), triglyceride (TG), fasting blood glucose (FBG) and glycosylated hemoglobin (HbAlc) were increased (Pï¼0.05). Compared with the low-altitude group, the expression levels of HIF-1α in diabetic patients at high-altitude and healthy people were increased significantly (Pï¼0.05), while the number of circulating EPCs was decreased significantly (Pï¼0.05), and the number of circulating EPCs in healthy people or the patients with type 2 diabetes without vascular complications was higher than that of patients with type 2 diabetes with vascular complications (Pï¼0.05). Conclusion: With the increase in altitude, the expression level of HIF-1α in type 2 diabetes mellitus(T2DM)patients is increased, and the number of circulating EPCs is decreased, which is closely related to the degree of vascular disease. Therefore, it is possible through transplantation of EPCs for high altitude T2DM patients to achieve the prevention and improvement of diabetic vascular complications.
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Altitud , Diabetes Mellitus Tipo 2 , Células Progenitoras Endoteliales , Subunidad alfa del Factor 1 Inducible por Hipoxia/metabolismo , Hemoglobina Glucada , HumanosRESUMEN
Long intergenic non-coding RNAs (lincRNAs) are long noncoding transcripts from the intergenic regions of annotated proteincoding genes. lincRNA cyclooxygenase 2 (Cox2) is an earlyprimary response gene regulated by the NFκB signaling pathway in macrophages. It was found that lincRNACox2 was significantly increased in patients with the Mycobacterium tuberculosis (M. tuberculosis) H37Ra strain infection and macrophages, using reverse transcription-quantitative PCR (RTqPCR). ELISA, western blotting and RTqPCR results indicated that the inflammatory response factors tumor necrosis factorα, interferonγ, interleukin6, Cox2 and inducible nitric oxide synthase were significantly increased in H37Ra infected macrophages. In addition, the inflammatory regulating proteins NFκB and Stat3 were significantly increased in H37Ra infected macrophages but decreased in lincRNACox2 knockdown macrophages infected with H37Ra. Moreover, the knockdown of lincRNACox2 increased the apoptotic rate of H37Ra infected macrophages and facilitated the proliferation of H37Ra. Collectively, the present results suggested that lincRNACox2 may be required for the activation of NFκB and Stat3, in order to regulate inflammatory responses involved in resistance to M. tuberculosis infection.
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Mycobacterium tuberculosis/patogenicidad , FN-kappa B/metabolismo , ARN Largo no Codificante/metabolismo , Tuberculosis/patología , Adulto , Apoptosis , Línea Celular , Ciclooxigenasa 2/genética , Ciclooxigenasa 2/metabolismo , Femenino , Humanos , Interferón gamma/genética , Interferón gamma/metabolismo , Macrófagos/citología , Macrófagos/metabolismo , Macrófagos/microbiología , Masculino , Persona de Mediana Edad , Óxido Nítrico Sintasa de Tipo II/genética , Óxido Nítrico Sintasa de Tipo II/metabolismo , Interferencia de ARN , ARN Largo no Codificante/antagonistas & inhibidores , ARN Largo no Codificante/genética , ARN Interferente Pequeño/metabolismo , Factor de Transcripción STAT3/metabolismo , Tuberculosis/inmunología , Tuberculosis/microbiología , Factor de Necrosis Tumoral alfa/genética , Factor de Necrosis Tumoral alfa/metabolismo , Adulto JovenRESUMEN
It is highly desirable to design high-efficiency stable and low-price catalysts in the electrocatalysis field. Herein, we reported a cobalt phosphide (Co2P)-loaded reduced graphene oxide (rGO) composite catalyst (rGO/Co2P) prepared via the convenient hydrothermal and H2 reduction methods. The rGO/Co2P catalyst reduced at 800 °C (rGO/Co2P-800) shows superior electrocatalytic activities for hydrogen evolution reaction and oxygen evolution reaction in 1.0 M KOH solution, achieving an overpotential of 134 and 378 mV, respectively, at a current density of 10 mA cm-2. Moreover, the catalyst can not only maintain stability for a long time in alkaline solution but also in acid media because of the protection of the rGO layers. The superior performance of this catalyst is attributed to the synergy between the carbon layer and transition-metal phosphides. The Co2P nanoparticles have a high degree of dispersion, which prevents agglomeration, thereby exposing more active sites. Moreover, rGO protects the exposed metal particles while providing more electroconductivity to the material. This work provides an efficient route for the development of bifunctional electrocatalysts with excellent performance and stability, which provides new ideas toward overall water splitting.